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Structure of 134176-18-4
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rel-Ethyl (1R,5S,6R)-2-oxobicyclo[3.1.0]hexane-6-carboxylate features a rigid bicyclic scaffold with defined stereochemistry, enabling precise control in asymmetric synthesis. The α-keto ester functionality supports direct functionalization and serves as a key intermediate in the construction of complex carbocyclic frameworks.
rel-Ethyl (1R,5S,6R)-2-oxobicyclo[3.1.0]hexane-6-carboxylate serves as a versatile bicyclic synthon for the construction of complex carbocyclic frameworks. Its strained cyclohexanone core enables efficient Michael additions and conjugate functionalizations, while the ester group facilitates selective transformations. Bench-stable and compatible with standard protecting group strategies, it functions reliably in multi-step synthesis of natural product analogs and medicinal chemistry libraries.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: